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The DING Family of Phosphate Binding Proteins in Inflammatory Diseases

机译:炎症性疾病中磷酸盐结合蛋白的丁家族

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摘要

Human paraoxonase 1 (hPON-1) is a protein that has been studied in relation to its antioxidant and anti-atherosclerotic properties. Despite extensive studies, the molecular mechanisms responsible for its functional properties remain unclear. During the last decade, a new partner of hPON-1 has been identified. Hidden for a long time because of a similar molecular weight with hPON-1, this protein, termed human phosphate-binding protein (HPBP), may contribute to the biological functions of hPON-1. Belonging to the DING protein, a sub-family of phosphate binding proteins (PBP or pstS), HPBP stabilizes hPON-1 and might prevent calcification of arteries in case of advance atherosclerosis. The role of other DING proteins in some calcification processes (i.e. nephrolithiasis) and the identification of HPBP in the atheroma plaque support this hypothesis. Nevertheless, the relevance of hPON-1/HPBP as well as the molecular determinants in atherosclerosis remains to be elucidated.
机译:人对氧基酶1(HPON-1)是已经与其抗氧化和抗动脉粥样硬化性能相关的蛋白质。 尽管研究广泛,负责其功能性质的分子机制仍然不清楚。 在过去十年中,已经确定了HPON-1的新伙伴。 由于HPON-1类似的分子量,这种蛋白质称为人磷酸盐结合蛋白(HPBP)的蛋白质,可能有助于HPON-1的生物功能。 属于丁蛋白,磷酸盐结合蛋白的亚族(PBP或PST),HPBP稳定HPON-1,并且可以防止动脉的钙化在前进的动脉粥样硬化。 其他丁蛋白在一些钙化过程中的作用(即肾状二病原体)和体育斑疹中HPBP的鉴定支持这一假设。 然而,HPON-1 / HPBP的相关性以及动脉粥样硬化中的分子决定簇仍有待阐明。

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